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Volumn 129, Issue 5, 2007, Pages 1278-1286

Boronic acid-based bipyridinium salts as tunable receptors for monosaccharides and α-hydroxycarboxylates

Author keywords

[No Author keywords available]

Indexed keywords

CARBOHYDRATES; CARBOXYLIC ACIDS; CHARGE TRANSFER; COMPLEXATION; CRYSTAL STRUCTURE; DYES; GROUND STATE; SUBSTITUTION REACTIONS;

EID: 33846850341     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja066567i     Document Type: Article
Times cited : (146)

References (95)
  • 16
    • 27644481443 scopus 로고    scopus 로고
    • Wilson, Darrell, M.; Block, J. Diabetes Technol. Ther. 2005, 7, 788-791.
    • (b) Wilson, Darrell, M.; Block, J. Diabetes Technol. Ther. 2005, 7, 788-791.
  • 34
    • 33846824097 scopus 로고    scopus 로고
    • In general, the term viologen refers to any diquaternized bipyridyl salt
    • In general, the term viologen refers to any diquaternized bipyridyl salt.
  • 55
    • 10444254749 scopus 로고
    • (f) Yoon, K. B. Chem. Rev. 1993, 93, 321-339.
    • (1993) Chem. Rev , vol.93 , pp. 321-339
    • Yoon, K.B.1
  • 67
    • 33846835725 scopus 로고    scopus 로고
    • It is proposed that the addition of boronic acids alters the electronics as well as the sterics of the viologens, thereby affecting their static and dynamic quenching constants. See refs 9b,g
    • It is proposed that the addition of boronic acids alters the electronics as well as the sterics of the viologens, thereby affecting their static and dynamic quenching constants. See refs 9b,g.
  • 68
    • 33846823427 scopus 로고    scopus 로고
    • All of the receptors were tested at this concentration. However, since the receptors have different quenching strengths and are used in molar excess relative to dye, the amount of the dye-receptor complex formed may vary for each receptor studied
    • All of the receptors were tested at this concentration. However, since the receptors have different quenching strengths and are used in molar excess relative to dye, the amount of the dye-receptor complex formed may vary for each receptor studied.
  • 69
    • 0031949249 scopus 로고    scopus 로고
    • It is likely that the sigmoidal binding behavior may occur as a result of the large excess of [BBV] relative to that of [HPTS]; see: Metzger, A.; Anslyn, E. V. Angew. Chem., Int. Ed. 1998, 37, 649-652.
    • (a) It is likely that the sigmoidal binding behavior may occur as a result of the large excess of [BBV] relative to that of [HPTS]; see: Metzger, A.; Anslyn, E. V. Angew. Chem., Int. Ed. 1998, 37, 649-652.
  • 70
    • 33846791768 scopus 로고    scopus 로고
    • The [BBV]/[HPTS] ratio is large (125) for all the receptors studied, but the sigmoidal binding curve shape is most pronounced for 3,3′-o-BBV.
    • (b) The [BBV]/[HPTS] ratio is large (125) for all the receptors studied, but the sigmoidal binding curve shape is most pronounced for 3,3′-o-BBV.
  • 71
    • 0037007704 scopus 로고    scopus 로고
    • Other glucose sensing systems that display binding constants not proportional to changes in fluorescence intensities include: (a) Cao, H, Diaz, D. I, DiCesare, N, Lakowicz, J. R, Heagy, M. D. Org. Lett. 2002, 4, 1503-1505
    • Other glucose sensing systems that display binding constants not proportional to changes in fluorescence intensities include: (a) Cao, H.; Diaz, D. I.; DiCesare, N.; Lakowicz, J. R.; Heagy, M. D. Org. Lett. 2002, 4, 1503-1505.
  • 77
    • 33846791172 scopus 로고    scopus 로고
    • For completeness, α-glucopyranose bound to 3,3′- o-BBV and unbound 3,3′-o-BBV, were also modeled and found to have similar minimized energies (see Supporting Information).
    • For completeness, α-glucopyranose bound to 3,3′- o-BBV and unbound 3,3′-o-BBV, were also modeled and found to have similar minimized energies (see Supporting Information).
  • 92
    • 33846824094 scopus 로고    scopus 로고
    • 11B spin-spin coupling, signals for carbons directly attached to boron are not observed.
    • 11B spin-spin coupling, signals for carbons directly attached to boron are not observed.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.